{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-09-17", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "197510", "product_res_number": "Z-1107-2023", "event_date_initiated": "2022-10-24", "event_date_posted": "2023-02-09", "recall_status": "Open, Classified", "res_event_number": "91338", "product_code": "OWB", "k_numbers": [ "K173736", "K200360" ], "product_description": "TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument Tracker, 6.5L, Model #605-3TX, Sterile.", "code_info": "Insight Base -5L - Lot #2206001, exp. 6/1/2025, UDI 00857088008431; Insight Base 6.5L - Lot #2202002, exp. 2/1/20024, UDI 00857088008448.", "firm_fei_number": "3014391847", "recalling_firm": "Trackx Technology Inc", "address_1": "437 Dimmocks Mill Rd Ste 28 437 Dimmocks Mill Rd", "address_2": "Ste 28", "city": "Hillsborough", "state": "NC", "postal_code": "27278-2379", "additional_info_contact": "Frederick Cole\n209-403-3160", "reason_for_recall": "The device is breaking and falling off the Nuvasive T-Handle with Hudson Adapter on certain Nuvasive XLIF instruments during surgery when malleted.", "root_cause_description": "Device Design", "action": "The recall was initiated via phone call on 10/24/2022 and 10/27/2022 (as well as subsequent in-person meetings) to two of the physicians who use the product in the affected application. The physicians were notified that the products can fragment when attached to a T-Handle and Nuvasive XLIF disectomy instruments while malleting and TrackX is limiting the use of those two bases to situations in the Nuvasive XLIF and Lateral Interbody procedures that do not require the malleting of the T-handle. The product is to be used in a limited manner and not on the Nuvasive T-Handle with Nuvasive XLIF Disectomy instruments.\n\nLetters dated 12/30/2022 began issuing via hand delivery or via DocuSign to all customers who have received the products. The letter informed the customer of the issue and said the IFU was revised with the application change and warning. The customer was informed that if they have further distributed or transferred the product to another location, they are to notify the recipients of the field action. A distribution list was provided to show the product that was shipped to the customer. An Acknowledgement and Receipt Form was enclosed along with the revised IFU (Warnings and Precautions section).", "product_quantity": "464 devices", "distribution_pattern": "US Nationwide distribution in the states of AZ, FL, LA, NC, PA, VA, WA, WI.", "openfda": { "k_number": [ "K221516", "K243376", "K231669", "K222625", "K040675", "K150967", "K241572", "K210900", "K243328", "K153244", "K123226", "K130893", "K210912", "K152697", "K030544", "K252099", "K160455", "K183109", "K091918", "K172574", "K160147", "K101833", "K052202", "K123508", "K210307", "K936180", "K213479", "K240465", "K190626", "K073543", "K220342", "K243646", "K051064", "K061163", "K234067", "K011292", "K213768", "K010435", "K251523", "K170909", "K230950", "K141979", "K111551", "K232344", "K162614", "K193230", "K111344", "K120282", "K201743", "K041931", "K200022", "K240199", "K251199", "K101868", "K203623", "K220409", "K122644", "K031637", "K182546", "K221335", "K042793", "K121444", "K233107", "K142708", "K100102", 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